8-Prenylkaempferol accelerates osteoblast maturation through bone morphogenetic protein-2/p38 pathway to activate Runx2 transcription

被引:26
作者
Chiou, Wen-Fei [1 ,2 ]
Lee, Chia-Hsin [3 ]
Liao, Jyh-Fei [3 ]
Chen, Chien-Chih [4 ]
机构
[1] Natl Res Inst Chinese Med, Taipei, Taiwan
[2] Natl Yang Ming Univ, Inst Tradit Med, Taipei 112, Taiwan
[3] Natl Yang Ming Univ, Inst Pharmacol, Taipei 112, Taiwan
[4] Hungkuang Univ, Dept Biotechnol, Taichung, Taiwan
关键词
Sophora flavescens; 8-Prenylkaempferol; Osteoblastogenesis; Bone morphogenetic protein-2; MESENCHYMAL STEM-CELLS; SOPHORA-FLAVESCENS; GENE-EXPRESSION; IN-VITRO; DIFFERENTIATION; KINASE; GROWTH; BETA; RUNX2/CBFA1; COMPONENTS;
D O I
10.1016/j.lfs.2010.12.009
中图分类号
R-3 [医学研究方法]; R3 [基础医学];
学科分类号
100103 [病原生物学]; 100218 [急诊医学];
摘要
Aims: In this study, we investigated the effect of 8-prenylkaempferol (8-PK), a prenyl-flavonoid isolated from Sophora flavescens. on osteoblast differentiation and maturation. Main methods: MC3T3-E1 cells were exposed to 8-PK and the cytotoxicity was assayed. Osteoblast differentiation and maturation were evaluated by analyzing alkaline phosphatase (ALP) activity and cell mineralization, respectively. RT-PCR and Western blot were executed to determine the effects of 8-PK on osteoblast differentiation-related gene expression and signaling pathway. Key findings: 8-PK significantly promoted ALP activity, up-regulated mRNA expressions of osteocalcin, osteopontin, and type I collagen, and induced bone nodules formation. Induction of differentiation by 8-PK was associated with increased bone morphogenetic protein (BMP)-2 expression, and sequentially up-regulated the phosphorylations of Smad1/5/8 and p38, and increased the nuclear translocation of runt-related transcription factor 2 (Runx2). Addition of BMP-2 antagonist noggin blocked 8-PK and recombinant mouse BMP-2-induced ALP activity. reconfirming that BMP-2 production is required in 8-PK-mediated osteoblast differentiation. Noggin also abrogated 8-PK evoked phosphorylations of Smad1/5/8 and p38, suggesting that BMP-2 signaling is required for p38 activation in 8-PK-treated cells. Application of p38 inhibitor SB203580 repressed not only 8-PK-mediated activation of ALP, but also the nuclear translocation of Runx2 and bone nodules formation. Significance: The present results suggested that BMP-2/p38/Runx2 pathways were involved in 8-PK-induced differentiation/maturation of MC3T3-E1 osteoblasts and firstly demonstrated that 8-PK might be a promising agent for inducing osteogenesis. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:335 / 342
页数:8
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